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Vitamin K

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Vitamin K1 (phylloquinone). Both contain a functional naphthoquinone ring and an aliphatic side chain. Phylloquinone has a phytyl side chain.
Vitamin K2 (menaquinone). In menaquinone the side chain is composed of a varying number of isoprenoid residues.

Vitamin K (K from "Koagulations-Vitamin" in German, Danish, Swedish and Norwegian[1]) denotes a group of lipophilic, hydrophobic vitamins that are needed for the posttranslational modification of certain proteins, mostly required for blood coagulation. Chemically they are 2-methyl-1,4-naphthoquinone derivatives.

Vitamin K2 (menaquinone, menatetrenone) is normally produced by bacteria in the intestines, and dietary deficiency is extremely rare unless the intestines are heavily damaged or are unable to absorb the molecule[citation needed].

Chemical structure

All members of the vitamin K group of vitamins share a methylated naphthoquinone ring structure, and vary in the aliphatic side chain attached at the 3-position (see figure 1). Phylloquinone (also known as vitamin K1) invariably contains in its side chain four isoprenoid residues, one of which is unsaturated.

Menaquinones have side chains composed of a variable number of unsaturated isoprenoid residues; generally they are designated as MK-n, where n specifies the number of isoprenoids.

It is generally accepted that the naphthoquinone is the functional group, so that the mechanism of action is similar for all K-vitamins. Substantial differences may be expected, however, with respect to intestinal absorption, transport, tissue distribution, and bio-availability. These differences are caused by the different lipophilicity of the various side chains, and by the different food matrices in which they occur.

Physiology

Vitamin K is involved in the carboxylation of certain glutamate residues in proteins to form gamma-carboxyglutamate residues (abbreviated Gla-residues). The modified residues are situated within specific protein domains called Gla domains. Gla-residues are usually involved in binding calcium. The Gla-residues are essential for the biological activity of all known Gla-proteins.[2]

At this time 14 human proteins with Gla domains have been discovered, and they play key roles in the regulation of three physiological processes:

The U.S. Dietary Reference Intake (DRI) for an Adequate Intake (AI) of Vitamin K for a 25-year old male is 120 micrograms/day. In 2002), it was found that to get maximum carboxilation (activation) of Osteocalcin, necessary to get calcium where it should be: one would have to get 1000 mcg of Vitamin K1. Like other liposoluble vitamins [vitamins A, D, E], vitamin K is stored in the fat tissue of the human body and a chronic overdose of vitamin K can harm the body and lead to hypervitaminosis. No Tolerable Upper Intake Level (UL) has been set[6]

Sources of Vitamin K

Vitamin K is found chiefly in leafy green vegetables, particularly the dark green ones such as spinach and kale; Brassica (e.g. cabbage, cauliflower, broccoli, and brussels sprouts) are also high in Vitamin K as are some fruits such as avocado and kiwifruit. By way of reference, two tablespoons of parsley contain 153% of the recommended daily amount of vitamin K.[7]. Some vegetable oils, notably soybean, contain vitamin K, but at levels that would require relatively large caloric consumption to meet the USDA recommended levels.[8]

Phylloquinone (vitamin K1) is the major dietary form of vitamin K.
Menaquinone-4 and Menaquinone-7 (vitamin K2) are found in meat, eggs, dairy [9] and natto[10]. MK-4 is synthesized by animal tissues, the rest (mainly MK-7) are synthesized by bacteria during fermentation. In natto 0% of Vitamin K is from MK-4 and in cheese 2-7%.[11]

Role in disease

Vitamin K-deficiency may occur by disturbed intestinal uptake (such as would occur in a bile duct obstruction), by therapeutic or accidental intake of vitamin K-antagonists or, very rarely, by nutritional vitamin K-deficiency. As a result, Gla-residues are inadequately formed and the Gla-proteins are insufficiently active. Lack of control of the three processes mentioned above may lead to the following: risk of massive, uncontrolled bleeding, cartilage calcification and severe malformation of developing bone, or deposition of insoluble calcium salts in the walls of arteries. The deposition of calcium in soft tissues, including arterial walls, is quite common, especially in those suffering from atherosclerosis, suggesting that Vitamin K deficiency is more common than previously thought.[5] Menaquinone, but not phylloquinone, intake is associated with reduced risk of CHD mortality, all-cause mortality and severe aortic calcification.[12][13][14]

In a cohort study in Germany (11319 men, mean follow-up time 8.6y), Menaquinone intake was associated with decreased incidence of advanced prostate cancer.[15]

Postmenopausal and elderly women in Thailand have high risk of Vitamin K2 deficiency, comparing to the normal value of young, reproductive females.[16] Current dosage recommendations for Vitamin K may be too low.[17]

Use on newborn babies

In some countries, injections of Vitamin K are routinely given to newborn babies. Vitamin K is used as prophylactic measure to prevent late-onset haemorrhagic disease (HDN). Since HDN is a relatively rare problem, many parents now choose for their babies not to have such an injection; most pediatricians, however, highly recommend the prophylactic dose for adequate protection.

Biochemistry

Discovery

In 1929, Danish scientist Henrik Dam investigated the role of cholesterol by feeding chickens a cholesterol-depleted diet.[18] After several weeks, the animals developed hemorrhages and started bleeding. These defects could not be restored by adding purified cholesterol to the diet. It appeared that - together with the cholesterol - a second compound had been extracted from the food, and this compound was called the coagulation vitamin. The new vitamin received the letter K because the initial discoveries were reported in a German journal, in which it was designated as Koagulationsvitamin. Edward Adelbert Doisy of Saint Louis University did much of the research that led to the discovery of the structure and chemical nature of Vitamin K.[19] Dam and Doisy shared the 1943 Nobel Prize for medicine for their work on Vitamin K. Several laboratories synthesized the compound in 1939.[20]

For several decades the vitamin K-deficient chick model was the only method of quantitating vitamin K in various foods: the chicks were made vitamin K-deficient and subsequently fed with known amounts of vitamin K-containing food. The extent to which blood coagulation was restored by the diet was taken as a measure for its vitamin K content. Three groups of physicians independently found this: Biochemical Institute, University of Copenhagen (Dam and Johannes Glavind), University of Iowa Department of Pathology (Emory Warner, Kenneth Brinkhous, and Harry Pratt Smith), and the Mayo Clinic (Hugh Butt, Albert Snell, and Arnold Osterberg). [21] The first published report of successful treatment with vitamin K of life-threatening hemorrhage in a jaundiced patient with prothrombin deficiency was made in 1938 by Smith, Warner, and Brinkhous.[22]

Function in the cell

The precise function of vitamin K was not discovered until 1974, when three laboratories (Stenflo et al.[23], Nelsestuen et al.[24], and Magnusson et al.[25]) isolated the vitamin K-dependent coagulation factor prothrombin (Factor II) from cows that received a high dose of a vitamin K antagonist, warfarin. It was shown that while warfarin-treated cows had a form of prothrombin that contained 10 glutamate amino acid residues near the amino terminus of this protein, the normal (untreated) cows contained 10 unusual residues which were chemically identified as gamma-carboxyglutamate, or Gla. The extra carboxyl group in Gla made clear that vitamin K plays a role in a carboxylation reaction during which Glu is converted into Gla.

The biochemistry of how Vitamin K is used to convert Glu to Gla has been elucidated over the past thirty years in academic laboratories throughout the world. Within the cell, Vitamin K undergoes electron reduction to a reduced form of Vitamin K (called Vitamin K hydroquinone) by the enzyme Vitamin K epoxide reductase (or VKOR).[26] Another enzyme then oxidizes Vitamin K hydroquinone to allow carboxylation of Glu to Gla; this enzyme is called the gamma-glutamyl carboxylase[27][28] or the Vitamin K-dependent carboxylase. The carboxylation reaction will only proceed if the carboxylase enzyme is able to oxidize Vitamin K hydroquinone to vitamin K epoxide at the same time; the carboxylation and epoxidation reactions are said to be coupled reactions. Vitamin K epoxide is then re-converted to Vitamin K by the Vitamin K epoxide reductase. These two enzymes comprise the so-called Vitamin K cycle.[29] One of the reasons why Vitamin K is rarely deficient in a human diet is because Vitamin K is continually recycled in our cells.

Warfarin and other coumarin drugs block the action of the Vitamin K epoxide reductase.[30] This results in decreased concentrations of Vitamin K and Vitamin K hydroquinone in the tissues, such that the carboxylation reaction catalyzed by the glutamyl carboxylase is inefficient. This results in the production of clotting factors with inadequate Gla. Without Gla on the amino termini of these factors, they no longer bind stably to the blood vessel endothelium and cannot activate clotting to allow formation of a clot during tissue injury. As it is impossible to predict what dose of Warfarin will give the desired degree of suppression of the clotting, Warfarin treatment must be carefully monitored to avoid over-dosing. See Warfarin.

Gla-proteins

At present, the following human Gla-containing proteins have been characterized to the level of primary structure: the blood coagulation factors II (prothrombin), VII, IX, and X, the anticoagulant proteins C and S, and the Factor X-targeting protein Z. The bone Gla-protein osteocalcin, the calcification inhibiting matrix gla protein (MGP), the cell growth regulating growth arrest specific gene 6 protein (Gas6), and the four transmembrane Gla proteins (TMGPs) the function of which is at present unknown. Gas6 can function as a growth factor that activates the Axl receptor tyrosine kinase and stimulates cell proliferation or prevents apoptosis in some cells. In all cases in which their function was known, the presence of the Gla-residues in these proteins turned out to be essential for functional activity.

Gla-proteins are known to occur in a wide variety of vertebrates: mammals, birds, reptiles, and fish. The venom of a number of Australian snakes acts by activating the human blood clotting system. Remarkably, in some cases activation is accomplished by snake Gla-containing enzymes that bind to the endothelium of human blood vessels and catalyze the conversion of procoagulant clotting factors into activated ones, leading to unwanted and potentially deadly clotting.

Another interesting class of invertebrate Gla-containing proteins is synthesized by the fish-hunting snail Conus geographus.[31] These snails produce a venom containing hundreds of neuro-active peptides, or conotoxins, which is sufficiently toxic to kill an adult human. Several of the conotoxins contain 2-5 Gla residues.[32]

Function in Bacteria

Many bacteria, such as Escherichia coli found in the large intestine, can synthesize Vitamin K2 (menaquinone),[33] but not Vitamin K1 (phylloquinone). In these bacteria, menaquinone will transfer two electrons between two different small molecules, in a process called anaerobic respiration.[34] For example, a small molecule with an excess of electrons (also called an electron donor) such as lactate, formate, or NADH, with the help of an enzyme, will pass two electrons to a menaquinone. The menaquinone, with the help of another enzyme, will in turn transfer these 2 electrons to a suitable oxidant, such fumarate or nitrate (also called an electron acceptor). Adding two electrons to fumarate or nitrate will convert the molecule to succinate or nitrite + water, respectively. Some of these reactions generate a cellular energy source, ATP, in a manner similar to eukaryotic cell aerobic respiration, except that the final electron acceptor is not molecular oxygen, but say fumarate or nitrate (In aerobic respiration, the final oxidant is molecular oxygen (O2) , which accepts four electrons from an electron donor such as NADH to be converted to water.) Escherichia coli can carry out aerobic respiration and menaquninone-mediated anaerobic respiration.

Carcinogenicity

Vitamin K substances are IARC Group 3 carcinogens. One study conducted in the United Kingdom in 1970 found a nearly two-fold increase of leukaemia in children administered synthetic Vitamin K1 phytomenadione intramuscularly[35], but later studies have failed to find whether Vitamin K is carcinogenic or not.[36][37][38][39]

References

  1. ^ Dam, Henrik (1935), "The Antihaemorrhagic Vitamin Of The Chick" (PDF), Biochemical Journal, XXIX (82): 1273–1285 {{citation}}: line feed character in |title= at position 29 (help)
  2. ^ Furie B, Bouchard BA, Furie BC (1999). "Vitamin K-dependent biosynthesis of gamma-carboxyglutamic acid". Blood. 93 (6): 1798–808. PMID 10068650.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Mann KG (1999). "Biochemistry and physiology of blood coagulation". Thromb. Haemost. 82 (2): 165–74. PMID 10605701.
  4. ^ Price PA (1988). "Role of vitamin-K-dependent proteins in bone metabolism". Annu. Rev. Nutr. 8: 565–83. doi:10.1146/annurev.nu.08.070188.003025. PMID 3060178.
  5. ^ a b Berkner KL, Runge KW (2004). "The physiology of vitamin K nutriture and vitamin K-dependent protein function in atherosclerosis". J. Thromb. Haemost. 2 (12): 2118–32. doi:10.1111/j.1538-7836.2004.00968.x. PMID 15613016.
  6. ^ Higdon (February 2008). "Vitamin K". Linus Pauling Institute, Oregon State University. Retrieved 2008-04-12.
  7. ^ Nutrition Facts and Information for Parsley, raw
  8. ^ Nutrition facts, calories in food, labels, nutritional information and analysis – NutritionData.com
  9. ^ Elder SJ, Haytowitz DB, Howe J, Peterson JW, Booth SL (2006). "Vitamin k contents of meat, dairy, and fast food in the u.s. Diet". J. Agric. Food Chem. 54 (2): 463–7. doi:10.1021/jf052400h. PMID 16417305. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  10. ^ Tsukamoto Y, Ichise H, Kakuda H, Yamaguchi M (2000). "Intake of fermented soybean (natto) increases circulating vitamin K2 (menaquinone-7) and gamma-carboxylated osteocalcin concentration in normal individuals". J. Bone Miner. Metab. 18 (4): 216–22. PMID 10874601.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  11. ^ "On the Trail of the Elusive X-Factor: Vitamin K2 Revealed".
  12. ^ Geleijnse JM, Vermeer C, Grobbee DE; et al. (2004). "Dietary intake of menaquinone is associated with a reduced risk of coronary heart disease: the Rotterdam Study". J. Nutr. 134 (11): 3100–5. PMID 15514282. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  13. ^ Erkkilä AT, Booth SL (2008). "Vitamin K intake and atherosclerosis". Curr. Opin. Lipidol. 19 (1): 39–42. doi:10.1097/MOL.0b013e3282f1c57f. PMID 18196985. {{cite journal}}: Unknown parameter |doi_brokendate= ignored (|doi-broken-date= suggested) (help)
  14. ^ Wallin R, Schurgers L, Wajih N (2008). "Effects of the blood coagulation vitamin K as an inhibitor of arterial calcification". Thromb. Res. 122: 411. doi:10.1016/j.thromres.2007.12.005. PMID 18234293.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  15. ^ Nimptsch K, Rohrmann S, Linseisen J (2008). "Dietary intake of vitamin K and risk of prostate cancer in the Heidelberg cohort of the European Prospective Investigation into Cancer and Nutrition (EPIC-Heidelberg)". Am. J. Clin. Nutr. 87 (4): 985–92. PMID 18400723. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  16. ^ Bunyaratavej N (2007). "[Experience of vitamin K2 in Thailand]". Clin Calcium (in Japanese). 17 (11): 1752–60. doi:CliCa071117521760. PMID 17982197. {{cite journal}}: Check |doi= value (help); Unknown parameter |doi_brokendate= ignored (|doi-broken-date= suggested) (help)
  17. ^ Adams J, Pepping J (2005). "Vitamin K in the treatment and prevention of osteoporosis and arterial calcification". Am J Health Syst Pharm. 62 (15): 1574–81. doi:10.2146/ajhp040357. PMID 16030366.
  18. ^ Dam H. The antihemorrhagic vitamin of the chick. Occurrence and chemical nature, Nature, 1935;135:652
  19. ^ MacCorquodale, DW, Binkley, SB, Thayer, SA, Doisy, EA, On the constitution of Vitamin K1, Journal of the American Chemical Society, 1939, 61:1928-1929
  20. ^ Fieser, LF, Synthesis of Vitamin K1, Journal of the American Chemical Society,1939, 61:3467-3475
  21. ^ Dam, Henrik (December 12, 1946). [The discovery of vitamin K, its biological functions and therapeutical application.] Nobel Prize lecture
  22. ^ Warner, ED, Brinkhous, KM, Smith, HP, Proceedings of the Society of Experimental Biology and Medicine, 1938, 37:628
  23. ^ Stenflo J, Fernlund P, Egan W, Roepstorff P., Vitamin K-dependent modifications of glutamic acid residues in prothrombin, Proceedings of the National Academy of Sciences, USA, 1974, 71:2730–3. PMID 4528109
  24. ^ Nelsestuen GL, Zytkovicz TH, Howard JB., The mode of action of vitamin K. Identification of gamma-carboxyglutamic acid as a component of prothrombin, Journal of Biological Chemistry, 1974, 249(19):6347-50. PMID 4214105
  25. ^ Magnusson S, Sottrup-Jensen L, Petersen TE, Morris HR, Dell A, Primary structure of the vitamin K-dependent part of prothrombin. FEBS Letters, 1974, 44(2):189-93. PMID 4472513
  26. ^ Oldenburg J, Bevans CG, Muller CR, Watzka M, Vitamin K epoxide reductase complex subunit 1 (VKORC1): the key protein of the vitamin K cycle, Antioxidants and Redox Signaling, 2006, 8(3-4):347-53. Review. PMID 16677080
  27. ^ Suttie JW, Vitamin K-dependent carboxylase, Annual Review of Biochemistry,1985, 54:459-77. Review. PMID 3896125
  28. ^ Presnell SR, Stafford DW, The vitamin K-dependent carboxylase, Thrombosis and Haemostasis, 2002, 87(6):937-46. Review. PMID 12083499
  29. ^ Stafford DW, The vitamin K cycle, Journal of Thrombosis Haemostasis, 2005, (8):1873-8. Review. PMID 16102054
  30. ^ Whitlon DS, Sadowski JA, Suttie JW, Mechanisms of coumarin action: significance of vitamin K epoxide reductase inhibition, Biochemistry, 1978, 17:1371–7. PMID 646989
  31. ^ Terlau H, Olivera BM. Conus venoms: a rich source of novel ion channel-targeted peptides, Physiological Reviews, 2004, 84(1):41-68. Review. PMID 14715910
  32. ^ Buczek O, Bulaj G, Olivera BM, Conotoxins and the posttranslational modification of secreted gene products, Cell and Molecular Life Sciences, 2005, 62(24):3067-79. Review. PMID:16314929
  33. ^ Bentley, R, Meganathan, R., Biosynthesis of Vitamin K (menaquinone) in Bacteria, Bacteriological Reviews, 1982, 46(3):241-280. Review.
  34. ^ Haddock, BA, Jones, CW, Bacterial Respiration, Bacteriological Reviews, 1977, 41(1):74-99. Review.
  35. ^ Vitamin K: controversy? what controversy?
  36. ^ "Controversies concerning vitamin K and the newborn. American Academy of Pediatrics Committee on Fetus and Newborn". Pediatrics. 112 (1 Pt 1): 191–2. 2003. PMID 12837888.
  37. ^ Fear NT, Roman E, Ansell P, Simpson J, Day N, Eden OB (2003). "Vitamin K and childhood cancer: a report from the United Kingdom Childhood Cancer Study". Br. J. Cancer. 89 (7): 1228–31. doi:10.1038/sj.bjc.6601278. PMID 14520451.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  38. ^ von Kries R (1999). "Oral versus intramuscular phytomenadione: safety and efficacy compared". Drug Saf. 21 (1): 1–6. PMID 10433349.
  39. ^ "IARC Monograph volume 76" (PDF). Retrieved 2008-03-07.

Further reading

  • Dam, H., Researches in Vitamin K, In: Pespectives in Biological Chemistry (RE Olson, ed.), Marcel Dekker, 1970. The Nobel Prize winner recounts the history of the discovery of Vitamin K.
  • Suttie, J.W., Vitamin K, In: Handbook of Lipid research: The fat-soluble vitamins (HF DeLuca, ed.), Plenum Press, 1978. Outstanding review of Vitamin K research from 1930-1978 by one of the leaders in the field.
  • David A. Bender, Nutritional biochemistry of the vitamins, Cambridge University Press, 2003
  • G. F. M. Ball, Vitamins: their role in the human body, Blackwell Science, 2004
  • Gerald F. Combs, The vitamins: fundamental aspects in nutrition and health, Academic Press, 1998